Linked Data
ClinVar Variation Id:
478476
dbSNP Id:
rs373906923
ExAC:
3:52404527 G / A
gnomAD v2:
3-52404527-G-A
gnomAD v3:
3-52370511-G-A
gnomAD v4:
3-52370511-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52370511G>A , CM000665.2:g.52370511G>A | GRCh38 |
| NC_000003.11:g.52404527G>A , CM000665.1:g.52404527G>A | GRCh37 |
| NC_000003.10:g.52379567G>A | NCBI36 |
| NG_052911.1:g.59193G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420323.7:c.6293G>A MANE Select | ENSP00000401514.2:p.Arg2098His | |
| ENST00000420323.6:c.6293G>A | ENSP00000401514.2:p.Arg2098His | |
| ENST00000486752.5:n.6554G>A | ||
| NM_015512.4:c.6293G>A | NP_056327.4:p.Arg2098His | |
| XM_011533577.1:c.6362G>A | XP_011531879.1:p.Arg2121His | |
| XM_017006129.1:c.6362G>A | XP_016861618.1:p.Arg2121His | |
| XM_017006130.1:c.6293G>A | XP_016861619.1:p.Arg2098His | |
| XM_017006131.1:c.6362G>A | XP_016861620.1:p.Arg2121His | |
| XM_017006132.1:c.6362G>A | XP_016861621.1:p.Arg2121His | |
| XM_017006133.1:c.6362G>A | XP_016861622.1:p.Arg2121His | |
| XR_001740098.1:n.9511G>A | ||
| XR_001740099.1:n.9511G>A | ||
| NM_015512.5:c.6293G>A MANE Select | NP_056327.4:p.Arg2098His |